Form 2 Annual Evaluation and Performance Measurement Report for

[NCEZID] Public Health Laboratory Testing for Emerging Antibiotic Resistance and Fungal Threats

Attachment 3b Form 2 Annual Evaluation and Performance Measurement Report for Bacterial Specimen Testing

OMB: 0920-1310

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OMB Control No.: 0920-1310

Expiration date: XX/XX/XXXX


Annual Progress Metric Measurement Report



Annually, each funded laboratory is required to report to CDC evaluation and performance measures. Data are used to indicate progress made toward program outcomes. These summary reports have to be submitted by email communication to [email protected] at the end of each funding year. Required performance measures are listed below.



1. Characterization of the clinical laboratory network in jurisdiction

2. Median and range (in days) from receipt of CRE/CRPA/CRAB isolates to communication of final mechanism testing and antibiotic susceptibility testing (AST) results to submitting laboratory

3. For results identified as a defined “alert” by CDC:

  1. Median and range (in days) to communicate test results with alert values to CDC and the HAI/AR program of originating jurisdiction

4. Number of laboratory personnel trained to proficiency in performing all tests in their AR Lab Network test directory

5. Proportion of isolates tested, and number of isolates tested by genera

6. Number of isolates transported upon request to CDC

7. Frequency and content of laboratory testing report or summaries shared with the HAI/AR program

8. For laboratories performing whole genome sequencing (WGS):

  1. Proportion of healthcare associated organism isolates tested by WGS that passed quality control in accordance with CDC testing protocols

9. Proportion of colonization swabs tested with results returned to submitter, in accordance with timeline per CDC guidance

10. Proportion of isolates tested for expanded drug susceptibility with results returned to submitter, in accordance with timeline per CDC guidance




Public reporting burden of this collection of information is estimated to average 240 minutes per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of information.  An agency may not conduct or sponsor, and a person is not required to respond to a collection of information unless it displays a currently valid OMB Control Number.  Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to CDC/ATSDR Reports Clearance Officer, 1600 Clifton Road NE, MS D-74, Atlanta, Georgia 30333; ATTN: PRA 0920-1310

File Typeapplication/vnd.openxmlformats-officedocument.wordprocessingml.document
AuthorTashayev, Valery (CDC/OID/NCEZID) (CTR)
File Modified0000-00-00
File Created2023-08-30

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